Comparison of the Adulthood Chronic Stress Effect on Hippocampal BDNF Signaling in Male and Female Rats

Mol Neurobiol. 2016 Aug;53(6):4026-4033. doi: 10.1007/s12035-015-9345-5. Epub 2015 Jul 21.

Abstract

Studies show that gender plays an important role in stress-related disorders, and women are more vulnerable to its effect. The present study was undertaken to investigate differences in the change in expression of brain-derived neurotrophic factor (BDNF), and its tyrosine intracellular kinase-activating receptor (TrkB) genes in the male and female rats' hippocampus (HPC) under chronic mild repeated stress (CMRS) conditions. In this experiment, male and female Wistar rats were randomly divided into two groups: the CMRS and the control group. To induce stress, a repeated forced swimming paradigm was employed daily for adult male and female rats for 21 days. At the end of the stress phase, elevated plus maze (EPM) was used for measuring the stress behavioral effects. Serum corticosterone level was measured by ELISA. BDNF and TrkB gene methylation and protein expression in the HPC were detected using real-time PCR and Western blotting. Chronic stress in the adolescence had more effects on anxiety-like behavior and serum corticosterone concentration in female rats than males. Furthermore, stressed female rats had higher methylation levels and following reduced protein expression of BDNF but not TrkB compared to stressed male rats. These findings suggest that in exposure to a stressor, sex differences in BDNF methylation may be root cause of decreased BDNF levels in females and may underlie susceptibility to pathology development.

Keywords: BDNF and TrKB; Chronic mild repeated stress; DNA methylation; Gender differences.

Publication types

  • Comparative Study

MeSH terms

  • Aging / metabolism*
  • Animals
  • Behavior, Animal
  • Blotting, Western
  • Brain-Derived Neurotrophic Factor / genetics
  • Brain-Derived Neurotrophic Factor / metabolism*
  • Chronic Disease
  • Corticosterone / blood
  • DNA Methylation / genetics
  • Female
  • Gene Expression Regulation
  • Hippocampus / metabolism*
  • Male
  • Maze Learning
  • Rats, Wistar
  • Receptor, trkB / genetics
  • Receptor, trkB / metabolism
  • Signal Transduction*
  • Stress, Psychological / blood
  • Stress, Psychological / genetics
  • Stress, Psychological / metabolism*
  • Swimming

Substances

  • Brain-Derived Neurotrophic Factor
  • Receptor, trkB
  • Corticosterone